Variant report
Variant | rs1723839 |
---|---|
Chromosome Location | chr11:73476723-73476724 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:73475127..73478054-chr11:73482525..73484326,2 | MCF-7 | breast: | |
2 | chr11:73468518..73473759-chr11:73476049..73479488,5 | K562 | blood: | |
3 | chr11:73475133..73477274-chr11:73489282..73491741,2 | MCF-7 | breast: | |
4 | chr11:73469480..73474305-chr11:73476302..73479488,4 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000175582 | Chromatin interaction |
ENSG00000256034 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10898944 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs11235903 | 0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs12293194 | 0.86[AFR][1000 genomes] |
rs1525750 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1525751 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1621654 | 0.89[AFR][1000 genomes] |
rs1624231 | 0.88[AMR][1000 genomes] |
rs1670548 | 0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1723834 | 0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1723838 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs1723842 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1723844 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1723845 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs1723846 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs1723849 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1792157 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1792195 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1792196 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1880642 | 0.83[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs1880643 | 0.83[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs1976914 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2037706 | 0.81[EUR][1000 genomes] |
rs2037709 | 0.92[EUR][1000 genomes] |
rs2056649 | 0.96[EUR][1000 genomes] |
rs2366944 | 0.92[EUR][1000 genomes] |
rs2444600 | 0.82[AFR][1000 genomes] |
rs2462617 | 0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2511263 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2511265 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2511269 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2515091 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs4548648 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs4551800 | 0.83[AFR][1000 genomes] |
rs4944026 | 0.92[EUR][1000 genomes] |
rs4944027 | 0.83[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs4944030 | 0.83[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs4944854 | 0.81[EUR][1000 genomes] |
rs4944857 | 0.92[EUR][1000 genomes] |
rs4944859 | 0.90[AFR][1000 genomes];0.96[EUR][1000 genomes] |
rs4944860 | 0.96[EUR][1000 genomes] |
rs4944864 | 0.90[EUR][1000 genomes] |
rs4944865 | 0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs6592528 | 0.81[EUR][1000 genomes] |
rs6592529 | 0.83[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs7396121 | 0.92[EUR][1000 genomes] |
rs7942515 | 0.92[EUR][1000 genomes] |
rs7950472 | 0.86[AFR][1000 genomes] |
rs940831 | 0.92[EUR][1000 genomes] |
rs9634024 | 0.90[AFR][1000 genomes];0.96[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530624 | chr11:73114283-73646329 | Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 55 gene(s) | inside rSNPs | diseases |
2 | nsv492091 | chr11:73285970-73844424 | Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 85 gene(s) | inside rSNPs | diseases |
3 | nsv1045149 | chr11:73314565-73581908 | Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
4 | nsv530641 | chr11:73358393-73638725 | Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
5 | nsv897912 | chr11:73436008-73477045 | Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
6 | esv3426251 | chr11:73461503-73538032 | Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:73472800-73477600 | Weak transcription | HSMMtube | muscle |
2 | chr11:73473000-73481400 | Weak transcription | Hela-S3 | cervix |
3 | chr11:73475600-73479800 | Weak transcription | K562 | blood |
4 | chr11:73476600-73477800 | Enhancers | Stomach Mucosa | stomach |